Oxidized divinyl oligoacene-bridged diruthenium complexes: bridged localized radical characters and reduced aromaticity in bridge cores.

A series of bimetallic ruthenium vinyl complexes 1-5 bridged by oligoacenes were synthesized and characterized in this study. Comparative cyclic voltammetry results from 1-5 indicated that the first oxidation potential decreased gradually with the extension of conjugate ligands. Upon oxidation to singly oxidized species 1+-5+, rather small ν(CO) changes in the infrared (IR) spectra and the characteristic bands of metal-to-ligand charge transfer absorptions in the near IR (NIR) region predicted via time-dependent DFT calculations suggested that strong bridged ligands participate in redox processes. NIR absorptions were not observed in complexes 4+ and 5+ possibly because of instability in their twisted and noncoplanar geometry. Electron paramagnetic resonance results and spin density distribution demonstrated that the bridged localized degrees of 1+-5+ successively increased with the extension of oligoacene from benzene to tetracene. Further comparative analysis of neutral molecules and monocations to the aromaticity and π-electron density of bridge cores indicated a step-by-step transformation process from an aromatic to quinoidal radical upon oxidation.